Anticotyledon factor: Competitive inhibitors of the action of dihydroconiferyl alcohol in stimulating gibberellic acid-induced lettuce hypocotyl elongation was written by Kamisaka, Seiichiro;Shibata, Kozo. And the article was included in Plant and Cell Physiology in 1977.Recommanded Product: 3-(3,4-Dimethoxyphenyl)propan-1-ol This article mentions the following:
The lettuce cotyledon factor, dihydroconiferyl alc., synergistically enhanced the stimulating effect of gibberellic acid (GA3) on hypocotyl elongation of decotylized lettuce seedlings. The action of dihydroconiferyl alc. was inhibited by 3-(3,4-dimethoxyphenyl)propanol, 3-(3-hydroxy-4-methoxyphenyl)propionic acid, methyl p-methoxycinnamate, trans-cinnamic acid, p-coumaric acid, ferulic acid, caffeic acid, and synapic acid. Kinetic studies with Lineweaver-Burk plots indicated that these compounds were competitive inhibitors of dihydroconiferyl alc. These inhibitors were termed anticotyledon factors. The action of dihydroconiferyl alc. was not influenced by phenylalanine, tyrosine, p-coumaryl alc., and coniferyl alc. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Recommanded Product: 3-(3,4-Dimethoxyphenyl)propan-1-ol).
3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.Recommanded Product: 3-(3,4-Dimethoxyphenyl)propan-1-ol
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem